EP1152027B1 - Polyolefinfilmzusammensetzungen mit Antibeschlageigenschaften - Google Patents

Polyolefinfilmzusammensetzungen mit Antibeschlageigenschaften Download PDF

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Publication number
EP1152027B1
EP1152027B1 EP01810412A EP01810412A EP1152027B1 EP 1152027 B1 EP1152027 B1 EP 1152027B1 EP 01810412 A EP01810412 A EP 01810412A EP 01810412 A EP01810412 A EP 01810412A EP 1152027 B1 EP1152027 B1 EP 1152027B1
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EP
European Patent Office
Prior art keywords
hydroxy
butyl
tert
film
bis
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Expired - Lifetime
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EP01810412A
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English (en)
French (fr)
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EP1152027A1 (de
Inventor
Anunay Gupta
David Devore
John James Mcnamara
Alessandro Zedda
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BASF Schweiz AG
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Ciba Spezialitaetenchemie Holding AG
Ciba SC Holding AG
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Priority to DK01810412T priority Critical patent/DK1152027T3/da
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04—Homopolymers or copolymers of ethene
    • C08L23/06—Polyethene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18—Manufacture of films or sheets
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
    • C08J2323/04—Homopolymers or copolymers of ethene
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31855—Of addition polymer from unsaturated monomers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31855—Of addition polymer from unsaturated monomers
    • Y10T428/31909—Next to second addition polymer from unsaturated monomers

Definitions

  • This invention relates to novel olefin polymer compositions which are resistant to fogging, especially when employed as a packaging film for moist products and as a greenhouse film for agricultural applications.
  • Agricultural films which are largely used in greenhouse culture or tunnel culture chiefly include soft ethylene resin films which are about 30 to 200 microns thick and which comprise, as a base resin, polyvinyl chloride (hereinafter abbreviated as PVC), branched low-density polyethylene (hereinafter abbreviated as LDPE), ethylene-vinyl acetate copolymers (hereinafter abbreviated as EVA), linear low-density polyethylene (hereinafter abbreviated as LLDPE), etc.
  • PVC polyvinyl chloride
  • LDPE branched low-density polyethylene
  • EVA ethylene-vinyl acetate copolymers
  • LLDPE linear low-density polyethylene
  • the atmosphere within greenhouses or tunnels surrounded by an agricultural film is saturated with water vapour which evaporates from the soil or plants, and the water vapour dropwise condenses on the inner surface of a cold film to cause fogging.
  • Water droplets on the film not only greatly reduce the incident sunlight due to irregular reflection but the droplets fall on the plants resulting in frequent occurrence of diseases.
  • antifog treatments on the inner surface of an agricultural film converting the film into an anti-stick water film and preventing adhesion of water droplets have been used thereby assuring transmission of sunlight into the greenhouse or tunnel, raising the soil temperature and air temperature within the greenhouse or tunnel, accelerating photosynthesis of the plants, accelerating healthy growth of the plants, and controlling the occurrence of plant diseases.
  • antifog treatments include incorporation of an anti-fogging agent (antifog additive) into a film-forming ethylene resin compound and coating of an anti-fogging agent on a film.
  • an anti-fogging agent anti-fogg additive
  • an anti-fogging film obtained by coating a soft plastic film with an anti-fogging agent has not yet been employed practically as an agricultural film for the following reasons.
  • soft plastic films for agricultural use generally have poor wettability and adhesion when coated with surface active agents or hydrophilic high polymeric substances which have been used as anti-fogging agents. This tendency is particularly conspicuous with soft ethylene resin films of low polarity, e.g., LDPE, EVA, and LLDPE films.
  • an anti-fogging agent is spray coated with a power atomiser onto a soft ethylene resin film
  • the anti-fogging agent needs to be used in a large quantity and this increases cost, and a large amount of time is required for spray coating operation. Further, spray coating cannot be effected uniformly with insufficient anti-fogging effects arising.
  • an anti-fogging agent is applied using a coater, etc.
  • a large quantity of a coating is consumed, and the coating speed cannot be increased, resulting in an increase of cost.
  • the coated anti-fogging agent is washed away together with running water droplets due to poor adhesion resulting in a very short life for the anti-fogging properties.
  • the coated film undergoes blocking due to the stickiness of the anti-fogging agent.
  • it has been impossible to retain anti-fogging effects in a stable manner for a long duration of at least 1 year, more desirably, several years.
  • Most of the state-of-the-art agricultural films exhibit anti-fogging properties for a period of only about 1 month.
  • Anti-fogging agents commonly incorporated into the films include non-ionic, anionic and cationic surface active agents.
  • coating type anti-fogging agents mainly comprising an inorganic hydrophilic colloidal substance and a hydrophilic organic compound have recently been developed as disclosed, e.g., in JP63-45432 and JP63-45717.
  • Suitable inorganic hydrophilic colloidal substances include colloidal silica, colloidal alumina, colloidal Fe(OH) 2 , colloidal Sn(OH) 4 , colloidal TiO 2 , colloidal BaSO 4 , and colloidal lithium silicate, with colloidal silica and colloidal alumina most generally used.
  • Suitable hydrophilic organic compounds include various non-ionic, anionic or cationic surface active agents; graft copolymers mainly comprising a hydroxyl-containing vinyl monomer unit and from 0.1 to 40% by weight of a carboxyl-containing vinyl monomer unit or a partial or complete neutralisation product thereof; and sulfo-containing polyester resins.
  • Coating type anti-fogging agents used with this new film type have markedly improved wettability and adhesion and coated agricultural films exhibiting anti-fogging properties for a duration of about a half year to about 1 year are provided.
  • Food products are often packaged in polymeric film for ease in handling by customers, to provide sanitary protection of the food product from the environment, to provide an easier and more economical wrapping than paper, or to provide a better view of the food product.
  • Various polymeric materials such as polyvinyl chloride, poly(ethylene/vinyl acetate) and irradiated polyethylenes have been used in the food wrap market with plasticized polyvinyl chloride (PVC) being widely used in the market.
  • PVC plasticized polyvinyl chloride
  • Freshly cut meat and vegetables are often packaged in these films, and certain properties are desired of the film for it to perform satisfactorily as a food overwrap.
  • film used in this application should have good "see through" clarity so the product can be viewed.
  • High gloss is desired to add "sparkle” to the packages for aesthetic appeal to the customers.
  • these food products As these food products are packaged, they generally experience a temperature change from where they are packaged to where they are stored or sold. This temperature change can cause the formation of water droplets on the inside surface of the film (commonly called “fog”). These water droplets are usually objectionable because they hinder the view of the food products from the consumer and can cause spoilage, particularly to certain vegetables.
  • an antifog agent is often added to the film. The antifog agents reduce the surface tension of the water and cause the water to form a continuous sheet, which is then transparent.
  • PVC polyvinylchloride
  • U.S. Pat. No. 5,262,233 discloses agricultural films which may have incorporated therein an anti-fogging agent which may be a poly(ethylene oxide) of a long chain alcohol.
  • WO91/04853 describes a polymeric composition having enhanced surface energy comprising e. g. a compound of the formula RO-(CH 2 CH 2 O) 9 R.
  • Atmer® 502 is described in a September, 1998 data sheet as having long-lasting antifog properties in LDPE agricultural film.
  • Atmer® 502 an ethoxylated ether, is a trademark of ICI Americas.
  • the present invention pertains to polyolefin film compositions with anti-fogging properties comprising comprising
  • polystyrene resins examples are:
  • Preferred polyolefins are polyethylene or polypropylene and their copolymers with mono- and diolefins.
  • the ethylene polymers of the present invention are those that are characterised as having a melt index or melt flow value, in the range of about 0.01 to about 20 gms./10 min. as measured by ASTM-D-1238, condition E, and a density in the range of about 0.9 to about 0.96 gms./cc.
  • a free-radical initiator e.g. peroxy compounds
  • LDPE low density polyethylene
  • co-ordination catalyst e.g. a "Ziegler-type catalyst
  • LLDPE linear low density polyethylenes
  • ethylene polymers which contain other comonomers, such as acrylic acid, methacrylic acid, alkyl acrylates, vinyl esters, and carbon monoxide.
  • monomers which contain oxygen atoms, are employed using a free-radical initiator, but are not very well suitable when co-ordination catalysts are employed.
  • the co-ordination catalysts which generally contain metal-carbon bonds, are usually poisoned or deactivated by compounds containing oxygen-carbon bonds or hydrogen-oxygen bonds when employed in quantities such as are involved in copolymerisation thereof.
  • copolymerisation of ethylene with the higher hydrocarbon olefins is best done using a co-ordination type catalyst.
  • the ethylene polymer be of the LLDPE variety, especially those which have a melt flow value in the range of about 0.1-10 and enough comonomer units to give a density in the range of about 0.9 to about 0.935 g/cc, such comonomer units being an aliphatic hydrocarbon olefin of from 4 to 8 carbon atoms, including isomers in that range.
  • LLDPE polymers are recognised in the art as having excellent strength, resistance to tear propagation as shown by Dart Impact and Elmendorf Tear, and exhibit good resistance to tearing or puncturing when stressed against articles having protuberances. This preference for the LLDPE variety is especially important in food packaging applications and most especially in packaging of red meat.
  • the fog-resistant films of this invention are prepared by producing a film of a formulation comprising a polyolefin having incorporated therein an A-B diblock copolymer antifog agent.
  • These copolymers are of the structure CH 3 CH 2 (CH 2 CH 2 ) a CH 2 CH 2 (OCH 2 CH 2 ) b OH where a is 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24 or 25 and b is 1 to 10.
  • Preferred are compositions comprising an A-B diblock compound where a is 13 and b is 2.5.
  • the values for the indices a and b are average values.
  • the polymer formulations of the present invention preferably contain an amount of the antifog agent in the range of about 0.1% to about 4%, most preferably an amount in the range of about 0.5% to about 3%, based on the overall weight of the formulation.
  • compositions may comprise other known antifog additives, such as alkoxylated ethers, e.g. Atmer® 502, sorbitan esters, e.g. Atmer® 103, other known non-ionic, anionic and cationic surface active agents as disclosed in the foregoing U.S. Patents, e.g., polyoxyalkylene fatty acid esters, alkoxylated phenols, mixed mono-, di-, or triglycerides, fatty acid esters of polyhydroxy alcohols, other polyalkoxylated compounds and the like.
  • Atmer® is a trademark of ICI Americas.
  • PCT application PCT/EP 01/00694 filed Jan. 23, 2001, incorporated herein by reference, discloses plastic films for food protection that comprise ultraviolet light absorbers.
  • the present polyolefin films with fog resistance may also contain further appropriate additives such as ultraviolet light absorbers, hindered amine light stabilisers, antioxidants, processing aids and other additives as disclosed in PCT application PCT/EP 01/00694.
  • compositions of the invention may optionally also contain from about 0.01 to about 10%, preferably from about 0.025 to about 5%, and especially from about 0.1 to about 3% by weight of various conventional stabiliser coadditives, such as the materials listed below, or mixtures thereof.
  • Alkylated monophenols for example,
  • esters of ⁇ -(3,5-di-tert-butyl-4-hydroxyphenyl)-propionic acid with monohydric or polyhydric alcohols for example,
  • esters of ⁇ -(5-tert-butyl-4-hydroxy-3-methylphenyl)-propionic acid with monohydric or polyhydric alcohols for example,
  • the mixing of the antifog agents into the polyolefin is done by mixing it into molten polymer by commonly used techniques such as roll-milling, mixing in a Banbury type mixer, or mixing in an extruder barrel and the like.
  • the heat history time at which held at elevated temperature
  • the antifog agent can also be added substantially simultaneously or sequentially with any other additives (colorants, tackifiers, slip agents, block agents, and the like) which may be desired in certain instances.
  • the antifog agents may also be preblended with other additives and the blend then added to the polymer. It is contemplated that in some instances these antifog agents should have the additional benefit of aiding the other additives to become more easily or evenly dispersed or dissolved in the polyolefin.
  • concentrated masterbatches of polymer/agent blends which are subsequently blended, as portions, to additional quantities of polymer to achieve the final desired formulation.
  • the masterbatch, or the neat additives may be injected into freshly prepared polymer while the polymer is still molten and after it leaves the polymerisation vessel or train, and blended therewith before the molten polymer is chilled to a solid or taken to further processing. It is within the purview of the present invention to employ blends or alloys of olefin polymers, whether they be of the above described LDPE, LLDPE, HDPE or other olefin polymers or copolymers made using a free-radical initiator or a co-ordination catalyst.
  • Polypropylene is an example of an olefin polymer made using a co-ordination catalyst (e.g. the well-known Ziegler or Natta catalysts or variations thereof) yet which inherently exhibits a low density compared to polyethylene.
  • polybutene or polyisobutylene is an effective tackifier or cling agent when mixed in polyethylene. In packaging processes, good cling properties are desirable in instances wherein the film is expected to cling to itself until pulled apart or until heat-sealed, as the case may be.
  • the polybutenes or polyisobutylenes usually employed for this purpose are generally used in small quantities of only a few percentage points of the total and are usually of low or relatively low molecular weight, having weight average mol weights in the range of from several hundred to a few thousand.
  • tackifiers are preferred in certain of the formulations contemplated as being within the purview of the present invention, especially in meat packaging (and the like) where it is desired that substantially no liquid leaks occur during the packaging operation until heat-sealed, or during shipping, storage, and handling after being heat-sealed.
  • films of polyolefins is well-known and includes the techniques of casting films as thin sheets through narrow slit dies, and the blown-film technique wherein an extruded tube of molten polymer is inflated to the desired "bubble" diameter and/or film thickness before being cooled and collected or further processed.
  • These present formulations are also suitable in coextrusion fabrication of films wherein two or more films comprise a multi-layer structure.
  • the antifog agents of the present invention can exude through an adjacent film layer which does not contain the antifog agent, thereby rendering the adjacent layer resistant to fogging.
  • the invention comprises a composition of a polyolefin resin and additives to form a film suitable for a red meat overwrap.
  • Polyolefin resins have the needed strength, optical, and gas permeability properties required for this market. However, they lack the wettability required to prevent moisture droplet formation in the package at lower temperatures.
  • anti-fogging agents such as mono- and diglycerides
  • plasticized PVC film were tried in polyolefin resins.
  • additives were not as effective in polyolefin resins as they were in plasticized PVC film.
  • the lack of plasticizers in polyolefin films might contribute to the difference observed in anti-fogging agents' behaviour.
  • Anti-fogging agents must be able to exude to the surface of the film where they can be effective, but not be abraded from the surface of the film. Anti-fogging agents that can be easily removed by water or by abrasion from the surface of the film are not desirable because the anti-fogging agents could flavour the meat, and the film would not be fog resistant.
  • the invention comprises the unique composition of an polyolefin resin and an effective anti-fogging agent that is not easily abraded from the surface of the film.
  • the use for this mixture of polyolefin resin and anti-fogging agent can be in food overwrap (meat, vegetables, etc.), greenhouse film, or other applications where a clear film with wettability or non-fogging is needed.
  • This invention differs from the widely used PVC red meat overwrap and produce wrap in that the base resin is a polyolefin instead of polyvinyl chloride resin.
  • Polyolefin resin has the advantage of not requiring plasticizers (e.g. dioctyl phthalate) such as required and used in PVC films.
  • Antifog agents perform differently in the two different classes of resin. Due to the plasticizers in PVC film, antifog agents are not as easily washed off the surface of the film. Thus, not all antifog agents that work in plasticized PVC film will work in polyolefin resin films.
  • the present invention incorporates the anti-fogging agent within the resin instead of applying it as a coating.
  • the incorporation of the additive into the resin is less expensive, less labour intensive, and more consistent than coatings applied to the surface of the film.
  • the present invention utilises anti-fogging agents that maintain their anti-fogging ability on the surface of the film even when the film has experienced abrasion. This aspect is important during the wrapping of food products so as to prevent the food products from absorbing the anti-fogging agent and to maintain the wettability of the film in the package.
  • the present invention allows the antifog agents to be incorporated into the resin, and the resin made into film by standard techniques with no additional treatment needed. No irradiation or heat ageing is necessary to cause the antifog agent to exude to the surface of the film where it is then effective. The antifog agents exude to the surface of the film within approximately 48 hours after fabrication.
  • polyolefin films of this invention with antifog properties are advantageously used for greenhouse films and for films used for food packaging applications.
  • Films are evaluated according to the hot fog test: A 250 mL glass beaker, containing about 50 mL of water and covered with the film to be evaluated, is immersed to about 1 ⁇ 2 of its height in a water bath at 60°C. Films are observed at defined intervals from the start of the experiment and a conventional notation ranging from A to E is assigned. Results are in Table 1. Rating for Hot fog Tests: Description Performance Rating Comments An opaque layer of small fog droplets None A Zero visibility, poor light transmission An opaque layer of large droplets None B Zero visibility, poor light transmission A complete layer of large dripping transparent droplets Poor C Poor visibility, lens effect, Randomly scattered large transparent droplets Fair D Discontinuous film of water Few small or large transparent droplets Good D/E Disc.
  • Additives are of the formula CH 3 CH 2 (CH 2 CH 2 ) a CH 2 CH 2 (OCH 2 CH 2 ) b OH, and the indices a and b are average values and refer to this formula.
  • antifog additives of the present invention provide superior long lasting results.
  • Example 1 is repeated to obtain formulations containing 1 or 2 % by weight of the additives of Table 2; films of about 75 ⁇ m are obtained.
  • Additives are of the formula CH 3 CH 2 (CH 2 CH 2 ) a CH 2 CH 2 (OCH 2 CH 2 ) b OH, and the indices a and b are average values and refer to this formula.
  • antifog additives of the present invention provide superior long lasting results.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Protection Of Plants (AREA)
  • Greenhouses (AREA)
  • Wrappers (AREA)
  • Laminated Bodies (AREA)

Claims (7)

  1. Beschlagbeständige Polyolefinfilm-Zusammensetzung, umfassend
    (a) einen Polyolefinfilm; und
    (b) eine Verbindung der Formel CH3CH2(CH2CH2)aCH2CH2(OCH2CH2)bOH,
    worin a für 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24 oder 25 steht, und b für 1 bis 10 steht.
  2. Zusammensetzung gemäß Anspruch 1, worin b für 1, 2, 3, 4, 5, 6, 7, 8, 9 oder 10 steht.
  3. Zusammensetzung gemäß Anspruch 1, worin das Polyolefin Polyethylen ist.
  4. Zusammensetzung gemäß Anspruch 1, worin die Komponente (b) eine Verbindung der Formel CH3CH2(CH2CH2)13CH2CH2(OCH2CH2)2,5OH ist.
  5. Zusammensetzung gemäß Anspruch 1, worin der Polyolefinfilm ein Gewächshausfilm ist.
  6. Zusammensetzung gemäß Anspruch 1, worin der Polyolefinfilm ein Film für die Nahrungsmittelverpackung ist.
  7. Verwendung einer Zusammensetzung gemäß Anspruch 1 als Verpackung für rotes Fleisch.
EP01810412A 2000-05-04 2001-04-26 Polyolefinfilmzusammensetzungen mit Antibeschlageigenschaften Expired - Lifetime EP1152027B1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DK01810412T DK1152027T3 (da) 2000-05-04 2001-04-26 Polyolefinfilmsammensætninger med permanente antidugegenskaber

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US20187100P 2000-05-04 2000-05-04
US201871P 2000-05-04

Publications (2)

Publication Number Publication Date
EP1152027A1 EP1152027A1 (de) 2001-11-07
EP1152027B1 true EP1152027B1 (de) 2004-09-15

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US (2) US6784235B2 (de)
EP (1) EP1152027B1 (de)
JP (1) JP2002012712A (de)
KR (1) KR100716601B1 (de)
CN (1) CN1171938C (de)
AR (1) AR035997A1 (de)
AT (1) ATE276308T1 (de)
BR (1) BR0101691B1 (de)
CA (1) CA2346198C (de)
DE (1) DE60105484T2 (de)
DK (1) DK1152027T3 (de)
ES (1) ES2227105T3 (de)
MX (1) MX235508B (de)
TW (1) TWI293974B (de)

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US20060167153A1 (en) * 2002-09-06 2006-07-27 Armin Schneider Film compositions with permanent anti-fog, anti-mist and anti-cloud properties
WO2005056661A2 (en) * 2003-12-08 2005-06-23 Huntsman Polymers Corporation Radiation resistant polypropylene useful in medical applications
CN101688028B (zh) * 2007-06-11 2012-07-18 巴斯夫欧洲公司 抗微生物聚烯烃和聚酯组合物
US7910646B1 (en) 2007-11-16 2011-03-22 Daniel Berg Molding composition with reduced coefficient of friction and improved release properties
CN103627069B (zh) * 2012-08-23 2016-06-08 中国石油天然气股份有限公司 高透明聚乙烯薄膜母料
US9777145B2 (en) 2013-12-20 2017-10-03 E. I. Du Pont De Nemours And Company Anti-fogging films based on ethylene copolymer compositions
CN106414053A (zh) * 2014-06-19 2017-02-15 阿格洛法士公司 用于包装农产品的组合物和方法
IL281313B2 (en) * 2014-11-20 2024-03-01 Cytec Ind Inc Stabilizers and methods of using them to protect organic polymeric materials against ultraviolet light and thermal decomposition
BR112018004216A2 (pt) * 2015-09-18 2018-09-25 Dow Global Technologies Llc filme de estufa de múltiplas camadas com desempenho antigotejamento superior
JP2018529006A (ja) * 2015-09-18 2018-10-04 ダウ グローバル テクノロジーズ エルエルシー 温室フィルムに使用される高性能滴下防止剤
DE102017216258A1 (de) 2017-09-14 2019-03-14 Mitsubishi Polyester Film Gmbh Beschichtete Polyesterfolie mit einer permanenten Antifog-Beschichtung und einer Transparenz von mindesten 93%
EP3681268B1 (de) 2017-09-14 2022-01-26 AB Ludvig Svensson Gewächshausabschirmung
US10428229B2 (en) 2017-12-28 2019-10-01 Industrial Technology Research Institute Aqueous coating material and method for manufacturing the same
DE102020213101A1 (de) 2020-10-16 2022-04-21 Mitsubishi Polyester Film Gmbh Ein- oder mehrschichtige Polyesterfolie mit einer permanenten Antifog-Beschichtung und einer Transparenz von mindestens 92%
JP2023546422A (ja) 2020-10-16 2023-11-02 エービー ルドヴィグ スヴェンソン 防曇効果を有する温室スクリーン

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JP2002012712A (ja) 2002-01-15
AR035997A1 (es) 2004-08-04
MX235508B (es) 2006-04-05
US7037964B2 (en) 2006-05-02
CN1323852A (zh) 2001-11-28
DE60105484D1 (de) 2004-10-21
DK1152027T3 (da) 2004-11-15
US20010047046A1 (en) 2001-11-29
ATE276308T1 (de) 2004-10-15
US6784235B2 (en) 2004-08-31
MXPA01004500A (es) 2004-09-10
KR100716601B1 (ko) 2007-05-10
TWI293974B (en) 2008-03-01
DE60105484T2 (de) 2005-10-13
BR0101691A (pt) 2001-12-18
CN1171938C (zh) 2004-10-20
US20040234801A1 (en) 2004-11-25
EP1152027A1 (de) 2001-11-07
KR20010102933A (ko) 2001-11-17
ES2227105T3 (es) 2005-04-01
CA2346198C (en) 2009-12-22
CA2346198A1 (en) 2001-11-04
BR0101691B1 (pt) 2010-09-21

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